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1227301-51-0

中文名称 1227301-51-0
英文名称 Philanthotoxin 74
CAS 1227301-51-0
分子式 C24H42N4O3.2HCl
更新日期 2025/05/16 15:53:10
分子量 471.08
MOL 文件 1227301-51-0.mol
1227301-51-0 结构式 1227301-51-0 结构式

基本信息

中文别名
化合物 T16524
PHILANTHOTOXIN 74二盐酸盐
化合物PHILANTHOTOXIN 74 盐酸盐
英文别名
PhTx 74。2HCl
PhTx-74 dihydrochloride
Philanthotoxin 74 dihydrochloride
Philanthotoxin 74 (hydrochloride)
Benzenepropanamide, N-[7-[(4-aminobutyl)amino]heptyl]-4-hydroxy-α-[(1-oxobutyl)amino]-, hydrochloride (1:2), (αS)-
所属类别
生物化工:激动剂抑制剂

物理化学性质

储存条件Inert atmosphere,Room Temperature
溶解度DMSO : 100 mg/mL (197.03 mM; Need ultrasonic)H2O : 50 mg/mL (98.51 mM; Need ultrasonic)
形态粉末
颜色White to light yellow

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS07
警示词警告
危险性描述H302-H315-H319-H335
1227301-51-0价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/02/08HY-104020A1227301-51-0
Philanthotoxin 74 dihydrochloride
1227301-51-01mg500元
2025/02/08HY-104020A1227301-51-0
Philanthotoxin 74 dihydrochloride
1227301-51-05mg800元
2025/02/08HY-104020A1227301-51-0
Philanthotoxin 74 dihydrochloride
1227301-51-010mM * 1mLin DMSO893元

常见问题列表

生物活性
Philanthotoxin 74 dihydrochloride (PhTx 74) 是 AMPAR 的拮抗剂; 抑制 GluR3 和 GluR1 的 IC50 值分别为263和296 nM。
靶点

IC50: 296 nM (GluR1), 296 nM (GluR1)

Ki: 0.29 μM (GluR5Q)

体外研究

Philanthotoxin 74 in the micromolar concentration range displays selective inhibition between the two major subtypes of GluA2R-containing AMPARs, GluA1/A2R and GluA2R/A3, when these are coexpressed with γ-2 in oocytes. Philanthotoxin 74 is reported to fully inhibit GluA1/A2R receptors when applied at a concentration of 500 μM while producing 10% inhibition at GluA2R/A3 receptors. Philanthotoxin 74, when tested at concentrations of 100 and 500 μM, displays pronounced channel block (more than 80%) of GluA1/A2R but minimal block (less than 10%) of GluA2R/A3. Oocytes expressing GluA2R alone that homomeric GluA2R is virtually inert to philanthotoxin 74 in the 0.1-300 μM concentration range, displaying less than 5% inhibition at the maximum tested concentration of 300 μM. Philanthotoxin 74 inhibits these receptors nonselectively, with IC 50 values of about 30 μM, in both the presence and absence of γ-2.

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